Canonical Allele Identifier: CA452781499

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510795A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189661A>G , CM000668.2:g.157189661A>G	GRCh38
NC_000006.11:g.157510795A>G , CM000668.1:g.157510795A>G	GRCh37
NC_000006.10:g.157552487A>G	NCBI36
NG_032093.1:g.416732A>G
NG_032093.2:g.416732A>G
NG_066624.1:g.418636A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3780A>G	ENSP00000055163.8:p.Gln1260=
ENST00000414678.8:c.3849A>G	ENSP00000412835.3:p.Gln1283=
ENST00000637015.2:c.4068A>G	ENSP00000489729.2:p.Gln1356=
ENST00000346085.10:c.3819A>G	ENSP00000344546.5:p.Gln1273=
ENST00000350026.10:c.3531A>G	ENSP00000055163.7:p.Gln1177=
ENST00000414678.7:c.2097A>G	ENSP00000412835.2:p.Gln699=
ENST00000635849.1:c.1260A>G	ENSP00000490948.1:p.Gln420=
ENST00000635957.1:c.894A>G	ENSP00000490385.1:p.Gln298=
ENST00000636930.2:c.3939A>G MANE Select	ENSP00000490491.2:p.Gln1313=
ENST00000636940.1:n.1936A>G
ENST00000637015.1:c.1307A>G
ENST00000637568.1:c.1221A>G
ENST00000637741.1:n.605A>G
ENST00000637810.1:c.1281A>G	ENSP00000489636.1:p.Gln427=
ENST00000637904.1:c.1440A>G	ENSP00000490550.1:p.Gln480=
ENST00000647938.1:c.3570A>G	ENSP00000498155.1:p.Gln1190=
ENST00000346085.9:c.3570A>G	ENSP00000344546.4:p.Gln1190=
ENST00000350026.9:c.3531A>G	ENSP00000055163.7:p.Gln1177=
ENST00000414678.6:c.2097A>G	ENSP00000412835.2:p.Gln699=
NM_017519.2:c.3531A>G	NP_059989.2:p.Gln1177=
NM_020732.3:c.3570A>G	NP_065783.3:p.Gln1190=
XM_005267069.3:c.3690A>G	XP_005267126.2:p.Gln1230=
XM_011535984.1:c.2769A>G	XP_011534286.1:p.Gln923=
XM_011535985.1:c.2589A>G	XP_011534287.1:p.Gln863=
XM_011535986.1:c.2349A>G	XP_011534288.1:p.Gln783=
XM_011535987.1:c.1968A>G	XP_011534289.1:p.Gln656=
XM_011535988.1:c.831A>G	XP_011534290.1:p.Gln277=
NM_001346813.1:c.3690A>G	NP_001333742.1:p.Gln1230=
NM_001363725.1:c.1440A>G	NP_001350654.1:p.Gln480=
XM_011535984.2:c.3900A>G	XP_011534286.2:p.Gln1300=
XM_011535988.3:c.831A>G	XP_011534290.1:p.Gln277=
XM_017011103.2:c.3801A>G	XP_016866592.1:p.Gln1267=
XM_017011104.1:c.3771A>G	XP_016866593.1:p.Gln1257=
XM_017011105.2:c.3741A>G	XP_016866594.1:p.Gln1247=
XM_017011106.2:c.3612A>G	XP_016866595.1:p.Gln1204=
XM_017011107.2:c.3591A>G	XP_016866596.1:p.Gln1197=
XR_002956289.1:n.3983A>G
NM_001363725.2:c.1440A>G	NP_001350654.1:p.Gln480=
NM_001371656.1:c.3819A>G	NP_001358585.1:p.Gln1273=
NM_001374820.1:c.3819A>G	NP_001361749.1:p.Gln1273=
NM_001374828.1:c.3939A>G MANE Select	NP_001361757.1:p.Gln1313=
NM_017519.3:c.3780A>G	NP_059989.3:p.Gln1260=